R2 Definitions Flashcards

(39 cards)

1
Q

Theoretical
yield

A

The maximum amount of product obtainable, assuming 100% of the limiting reactant is converted to product.

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2
Q

Determining Limit Reactant

A

Divide amount by the molar ratio

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3
Q

Rate of Reaction

A

Change in concentration of a particular reactant or product with time
In mol dm⁻³ s⁻¹

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4
Q

Rate formula

A

Δ[product]/Δt or - Δ[reactant]/Δt (emphasis on the negative)

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5
Q

Instantaneous Rate

A

Rate at t=0. Tangent at this point.

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6
Q

Rates Measuring Techqniues

A
  • Volume (needs to have gas particles)
  • Mass (needs gas but doesnt work well with light gases which will not really change overall mass (e.g. hydrogen))
  • pH (needs to be acid-base)
  • Conductivity (needs to have ions)
  • Change in transmission of light.
  • Change in concentration (measured through titration)
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7
Q

Gas method

A

2 ways:
1. Tube on the flask thats reacting with rubber stopper and this is connected to a plunger and displacement recorded.

  1. Fill and invert a burette and under water have a tube coming from the reaction flask into the burette which fills it - only works with low-soluble gases
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8
Q

Factors that impact rate

A

Concentration, temperature, surface area, and the presence of a catalyst

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9
Q

Energy Profile Axis

A

x - reaction coordinate, y - potential energy.

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10
Q

Energy Profile Steps

A

Reactants - EA - Transition state - drop - products.

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11
Q

Catalyst

A

Increases the rate of a chemical reaction without itself undergoing chemical change. Most catalysts work by providing an alternative route for the reaction that has a lower activation energy. Equal change to forward and reverse reactions.

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12
Q

Elementary Steps Molecularity

A

Unimolecular - An elementary step that involves a single reactant particle.

Bimolecular - An elementary step with two reactant particles. (e.g. NO + CO)

Termolecular - 3 but VERY UNLIKELY due to extremely low chance of 3 particles combining with sufficient E at the same time.

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13
Q

Overall Reaction Order is equal to

A

Power of all reactants added together.

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14
Q

How to determine order

A

Can only be determined experimentally through how concentration changes impact the rate.

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15
Q

What cannot be in a rate equation

A

An intermediate - figure out the rate equation of what makes it.

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16
Q

Can you prove a reaction mechanism from the formula?

A

No, you can only prove if it cannot be correct if the possible mechanisms fit the empirical findings - stoich and kinetic data match.

17
Q

Concentration-time graphs

A

Zero - y=-x
First - Negative exponential
Second - More harsh negative exponential

18
Q

Rate-concentration graph

A

Zero - Horizontal line
Second - y=x
Third - Positive exponential

19
Q

The two things the rate of a reaction is dependent on

A
  1. Concentration of reactants (not all if some are zero-order).
  2. k variable - can be changed by temperature changes/catalyst presence only.
20
Q

Arrhenius plot

A

In k = - (Ea)/(RT) + In A
This is a form of the equation for a straight line: y = mx + c
y axis - Ink
x axis - 1/T
Gradient - (-Ea)/(R)

21
Q

Formula to find Ea from the gradient

A

Ea (in J mol-1) = - gradient (in K) × 8.31 (R in J K-1 mol-1)

22
Q

Arrhenius Factor

A

The Arrhenius factor is a measure of the frequency of collisions and the orientation of reacting molecules. It represents the number of times reactants collide with the proper orientation to form products.

23
Q

Maxwell-Boltzmann Distribution Curves

A

Start at origin
y axis - Number of particles with a specific Kinetic Energy
x axis - Kinetic Energy

24
Q

5 things about equilibriums

A
  1. They are dynamic - reactions still occur.
  2. Only achieved in a closed
    system - no exchange of matter.
    3 The concentrations of reactants and products remain constant at
    equilibrium.
  3. Macroscopic properties do not change as they depend
    on the concentrations
  4. Equilibrium can be achieved from any start (e.g. all products or all reactants).
25
Equilibrium Constant (K)
For aA + bB ⇌ cC+ dD K=([D]^c * [D]^d)/([A]^a * [B]^b)
26
Reverse Reaction Equilibrium Constant
=1/K
27
Le Chataliers Principle
A system at equilibrium when subjected to a change will respond in such a way as to minimise the effect of the change.
27
How does concentration shift the equilibrium
Rate of the opposite reaction to whatever had its concentration increased will increase and a new equilibrium will be found further from the side which had concentration added. K does NOT change. On conc-time graph, when adding a specific reactant that reacant will have a sharp inc followed by a steady decrease (but new eq is higher than before) and other reactants will just decrease and be lower than before whilst products increase.
27
Changes that shift the equilibrium list
- Concentration - Pressure (gas) - Temperature
28
How does pressure shift the equilibrium.
If the number of molecules changes, then the equ shifts. An increase in pressure will favour the side with less molecules (determined by the molar ratio). E.g. CO + 2H₂ ⇌ CH₃OH has 3:1 particle ratio; therefore an increase in pressure will favour the forward reaction which will result in less molecules. K will not change.
29
How does temperature shift the equilibrium.
- Temperature changes will shift K. - The equilibrium will shift to favour the direction that counter-acts the temperature change (inc of temp=shift to endothermic, decrease of temp=shift to exothermic)
30
Exothermic
Reaction that releases energy (typically heat) into its surrounding, resulting in a negative ΔH.
30
Endothermic
Reaction that absorbs energy (typically heat) into its system, resulting in a positive ΔH.
31
How does a catalyst shift the equilibrium.
A catalyst decreases the activation energy for both the forward and reverse reactions equally, meaning both rates will increase to the same degree, maintaining the equilibrium and K.
32
Reaction Quotient (Q) and what it allows you to do (in relation to K)
A measure of the relative amounts of products and reactants present during a reaction at a particular point in time where the reaction is not at equilibrium. Allows you to predict which way the reaction will proceed to reach equilibrium.
33
ICE Method things to remember
- Use mols for ICE bit then convert to concentration - Balance equation and use mol ratios - If calculating concentrations from K and K is less than 10⁻³ then the x on reactants is removed. - Smallest x should be with co-efficient 1 and numbers with higher co-efficients in balanced will have higher x.
34
ΔG and what its sign means for equilibrium
Negative - reaction proceeds in the forwards direction. Positive - reaction proceeds in the negative direction. 0 - reaction is at equilibrium
35
ΔG and entropy at equilibrium
Gibs at minimum, entropy at maximum
36
Homologous and Heterogenous Chemical Reactions
Homo - All in same physical state Hetero - Different physical states.